Evidence map›Paper›PMID 24218615›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Global methylation state at base-pair resolution of the Caulobacter genome throughout the cell cycle.

Jennifer B Kozdon, Michael D Melfi, Khai Luong, Tyson A Clark, Matthew Boitano, Susana Wang, Bo Zhou, Diego Gonzalez, Justine Collier, Stephen W Turner and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
5.4field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

64 citing papers in PubMed, 117 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Comparison of CcrM-dependent methylation inJournal of bacteriology · 2024
    Article
  7. Article
  8. Comparison of CcrM-dependent methylation inbioRxiv : the preprint server for biology · 2024
    Article
  9. Article
  10. Comparison ofEpigenomes · 2023
    Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. DNA Methylation inmSystems · 2022
    Article
  16. DNA Methylation in Prokaryotes.Advances in experimental medicine and biology · 2022
    Article
  17. Review
  18. Article
  19. Article
  20. Article

4 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 2 countries.

Jennifer B KozdonDepartment of Developmental Biology, Stanford University, Stanford, CA 94305.
Michael D Melfi
Khai Luong
Tyson A Clark
Matthew Boitano
Susana Wang
Bo Zhou
Diego Gonzalez
Justine Collier
Stephen W Turner
Jonas Korlach
Lucy Shapiro
Harley H McAdams
Pacific Biosciences (United States) · USStanford University · USUniversity of Lausanne · CH

Funding

REGULATION OF DIFFERENTIATION IN CAULOBACTERR01GM032506 · NIGMS · YESHIVA UNIVERSITY · PI SHAPIRO, LUCILLE · 1985 to 2014
$7.1M
DEVELOPMENT CONTROL OF DNA REPLICATION IN CAULOBACTERR01GM051426 · NIGMS · STANFORD UNIVERSITY · PI SHAPIRO, LUCILLE · 1994 to 2013
$3.8M
Direct Single Base-Pair Real-Time DNA Methylation SequencingRC2HG005618 · NHGRI · PACIFIC BIOSCIENCES OF CALIFORNIA, INC. · PI TURNER, STEPHEN WHITFIELD · 2009 to 2010
$1.2M
NHGRI NIH HHS 1RC2HG005618-01NHGRI NIH HHS RC2 HG005618NIGMS NIH HHS R01 GM032506NIGMS NIH HHS R01 GM051426NIGMS NIH HHS R01-GM051426
6 · The paper itself

Abstract

The Caulobacter DNA methyltransferase CcrM is one of five master cell-cycle regulators. CcrM is transiently present near the end of DNA replication when it rapidly methylates the adenine in hemimethylated GANTC sequences. The timing of transcription of two master regulator genes and two cell division genes is controlled by the methylation state of GANTC sites in their promoters. To explore the global extent of this regulatory mechanism, we determined the methylation state of the entire chromosome at every base pair at five time points in the cell cycle using single-molecule, real-time sequencing. The methylation state of 4,515 GANTC sites, preferentially positioned in intergenic regions, changed progressively from full to hemimethylation as the replication forks advanced. However, 27 GANTC sites remained unmethylated throughout the cell cycle, suggesting that these protected sites could participate in epigenetic regulatory functions. An analysis of the time of activation of every cell-cycle regulatory transcription start site, coupled to both the position of a GANTC site in their promoter regions and the time in the cell cycle when the GANTC site transitions from full to hemimethylation, allowed the identification of 59 genes as candidates for epigenetic regulation. In addition, we identified two previously unidentified N(6)-methyladenine motifs and showed that they maintained a constant methylation state throughout the cell cycle. The cognate methyltransferase was identified for one of these motifs as well as for one of two 5-methylcytosine motifs.

Indexed as

AdenineBase SequenceCaulobacterCell CycleCloning, MolecularComputational BiologyCytosineDNA MethylationGene Expression Regulation, BacterialGenome, BacterialKineticsMolecular Sequence DataSequence Analysis, DNAAdenineCytosineDNA methylationmethylomeSMRT sequencing

Identifiers

PMID24218615
PMCPMC3845142
OpenAlexW1972921915

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.